Canonical Allele Identifier: CA1294881352
Gene: ZEB2 HGNC NCBI

Linked Data

dbSNP Id: rs1703132945

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144389815_144389823dup , CM000664.2:g.144389815_144389823dup GRCh38
NC_000002.11:g.145147382_145147390dup , CM000664.1:g.145147382_145147390dup GRCh37
NC_000002.10:g.144863852_144863860dup NCBI36
NG_016431.1:g.135571_135579dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*3124_*3132dup ENSP00000508434.1:n.*3124_*3132dup
ENST00000440875.6:c.2498_2506dup ENSP00000475553.3:p.Glu835_Ala836insGluArgGlu
ENST00000627532.3:c.3275_3283dup MANE Select ENSP00000487174.1:p.Glu1094_Ala1095insGluArgGlu
ENST00000636026.2:c.3230+45_3230+53dup ENSP00000490776.1:n.3230+45_3230+53dup
ENST00000636179.1:n.3244_3252dup
ENST00000636413.1:c.2939_2947dup ENSP00000490508.1:p.Glu982_Ala983insGluArgGlu
ENST00000636471.1:c.3350_3358dup ENSP00000490317.1:p.Glu1119_Ala1120insGluArgGlu
ENST00000636732.2:c.*2992_*3000dup ENSP00000490175.1:n.*2992_*3000dup
ENST00000636820.1:n.3375_3383dup
ENST00000637045.1:c.2939_2947dup ENSP00000490141.1:p.Glu982_Ala983insGluArgGlu
ENST00000637304.1:c.2939_2947dup ENSP00000490872.1:p.Glu982_Ala983insGluArgGlu
ENST00000638007.1:c.2939_2947dup ENSP00000490723.1:p.Glu982_Ala983insGluArgGlu
ENST00000638087.1:c.2939_2947dup ENSP00000490673.1:p.Glu982_Ala983insGluArgGlu
ENST00000638128.1:c.2498_2506dup ENSP00000490934.1:p.Glu835_Ala836insGluArgGlu
ENST00000639389.1:c.151+6591_151+6599dup ENSP00000492572.1:n.151+6591_151+6599dup
ENST00000647488.1:c.495_503dup ENSP00000494820.1:n.495_503dup
ENST00000675069.1:c.806_814dup ENSP00000502467.1:p.Glu271_Ala272insGluArgGlu
ENST00000303660.8:c.3272_3280dup ENSP00000302501.4:p.Glu1093_Ala1094insGluArgGlu
ENST00000409487.7:c.3275_3283dup ENSP00000386854.2:p.Glu1094_Ala1095insGluArgGlu
ENST00000419938.5:c.656-939_656-931dup ENSP00000394777.2:n.656-939_656-931dup
ENST00000539609.7:c.3203_3211dup ENSP00000443792.2:p.Glu1070_Ala1071insGluArgGlu
ENST00000558170.6:c.3275_3283dup ENSP00000454157.1:p.Glu1094_Ala1095insGluArgGlu
ENST00000627532.2:c.3275_3283dup ENSP00000487174.1:p.Glu1094_Ala1095insGluArgGlu
NM_001171653.1:c.3203_3211dup NP_001165124.1:p.Glu1070_Ala1071insGluArgGlu
NM_014795.3:c.3275_3283dup NP_055610.1:p.Glu1094_Ala1095insGluArgGlu
XM_006712881.2:c.3275_3283dup XP_006712944.1:p.Glu1094_Ala1095insGluArgGlu
XM_006712882.2:c.3275_3283dup XP_006712945.1:p.Glu1094_Ala1095insGluArgGlu
XM_011512231.1:c.3266_3274dup XP_011510533.1:p.Glu1091_Ala1092insGluArgGlu
XM_011512232.1:c.3254_3262dup XP_011510534.1:p.Glu1087_Ala1088insGluArgGlu
NM_014795.4:c.3275_3283dup MANE Select NP_055610.1:p.Glu1094_Ala1095insGluArgGlu
NM_001171653.2:c.3203_3211dup NP_001165124.1:p.Glu1070_Ala1071insGluArgGlu